rna-sequencing Downloads
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CD Genomics is a preeminent service provider specializing in exosome RNA sequencing and bioinformatics analysis. Based on cutting-edge platforms, we deliver end-to-end services with more usable reads from low-input RNA and in-depth scientific and technical support. https://rna.cd-genomics.com/exosomal-long-rna-seq.html ...
Lexogen is a biotech company that provides innovative solutions for one of the fastest developing technologies in the last decade – Next Generation Sequencing (NGS). The company’s main focus is the development of RNA sequencing technologies to resolve the complexity of the transcriptome. Lexogen was founded in 2007. The headquarters of the company are located in Vienna, Austria, and ...
Metabolic RNA sequencing combines labeling of newly synthesized RNA transcripts with RNA-Seq readout. Existing approaches utilize nucleotide derivatives such as 4-Thiouridine and biochemical pulldown to separate nascent and existing RNA for library preparation 1. These protocols are typically cost-, time-, and labor-intensive, require high amounts of RNA input, and often produce low signal ...
Tempus xE (version 2) is a whole exome next-generation sequencing assay that analyzes the entire coding region (exome) of the patient’s genome, combined with whole transcriptome RNA sequencing. Clinical sequencing is performed to 500x depth of coverage for tumor specimens and 150x for normal specimens for the clinically enhanced regions (648 genes). Non-enhanced regions are performed at ...
ByTempus
miR-ID assays are designed for miRNA analysis from total RNA samples Please send us your small RNA sequence or miRNA (miRbase) accession number. Pricing depends on complexity of the small RNA. Most commonly used miR-ID® assays cost $170. miR-ID® kit contents are sufficient for 100 RT reactions (20 ul each) and 300 PCR reactions (20 ul ...
To support medical research and translation, CD Genomics provides a full range of sequencing/microarray-based approaches including gene expression profiling, RNA-seq, whole-genome sequencing (WGS), whole-exome sequencing (WES), epigenomics, and single-cell sequencing for detecting tumour heterogeneity. ...
To support medical research and translation, we provide a full range of sequencing/microarray-based approaches including gene expression profiling, RNA-seq, whole-genome sequencing (WGS), whole-exome sequencing (WES), epigenomics, and single-cell sequencing for detecting tumor heterogeneity. ...
To support medical research and translation, CD Genomics provides a full range of sequencing/microarray-based approaches including gene expression profiling, RNA-seq, whole-genome sequencing (WGS), whole-exome sequencing (WES), epigenomics, and single-cell sequencing for detecting tumour heterogeneity. https://www.cd-genomics.com/Gene-Expression-Profiling-Microarray-Service.html ...
Whole transcriptome RNA sequencing allows for the analysis of fusion genes with potential clinical utility that currently cannot be detected using the limited genomic coverage of targeted NGS panels. Additionally, some clinical cancer testing labs are evaluating whole transcriptome panels for improved diagnostic yields and clinical utilization for NGS-based tumor profiling test reimbursements. ...